A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439077



Internal ID22181897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89059325..89059438hg38UCSC Ensembl
chr9:91674240..91674353hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214460
Supporting Variants
SamplesHG00514
Known GenesSHC3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14439077
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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